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Catalog Number:
39917
CAS Number:
365564-10-9
2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
3,4-Dimethoxyphenylboronic acid pinacol ester, 1,2-Dimethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
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Product Information

2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention for its unique properties and applications in organic synthesis and medicinal chemistry. This compound, often utilized as a reagent in cross-coupling reactions, facilitates the formation of carbon-carbon bonds, making it invaluable in the development of complex organic molecules. Its ability to stabilize reactive intermediates enhances reaction efficiency, which is particularly beneficial in pharmaceutical research and development, where time and precision are critical.

In addition to its synthetic utility, 2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane has shown promise in the field of materials science, particularly in the synthesis of advanced polymers and nanomaterials. Researchers appreciate its ease of use and the high yields it provides in various reactions. The compound's unique structural features allow for selective functionalization, making it an attractive option for those looking to innovate in both academic and industrial settings.

Synonyms
3,4-Dimethoxyphenylboronic acid pinacol ester, 1,2-Dimethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
CAS Number
365564-10-9
Purity
≥ 98% (GC)
Molecular Formula
C14H21BO4
Molecular Weight
264.13
MDL Number
MFCD05863909
PubChem ID
15906195
Melting Point
85 - 89 ?C
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,4-Dimethoxyphenylboronic acid pinacol ester, 1,2-Dimethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
CAS Number
365564-10-9
Purity
≥ 98% (GC)
Molecular Formula
C14H21BO4
Molecular Weight
264.13
MDL Number
MFCD05863909
PubChem ID
15906195
Melting Point
85 - 89 ?C
Appearance
White to off white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(3,4-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, enabling the formation of complex molecular structures through cross-coupling reactions, which are essential for developing new pharmaceuticals.
  • Material Science: It is applied in the creation of advanced materials, particularly in the development of polymers and nanomaterials, enhancing properties like strength and thermal stability.
  • Medicinal Chemistry: The compound plays a crucial role in drug design, particularly in the synthesis of boron-containing compounds that exhibit biological activity, potentially leading to new therapeutic agents.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, contributing to the development of more effective pesticides and herbicides that target specific pests while minimizing environmental impact.
  • Analytical Chemistry: This chemical is employed in various analytical techniques, such as chromatography, to improve the separation and detection of complex mixtures, aiding in quality control and research applications.

Citations